Novel bio-mediated Ag/Co3O4 nanocomposites of different weight ratios using aqueous neem leaf extract: Catalytic and microbial behaviour

An environmentally safe, economically, fast, and green synthetic approach was presented in this work for the fabrication of Ag-NP, Co₃O₄-NP and different weight ratio of Ag/Co₃O₄-NC. The synthesized samples were characterized by Fourier-transform infrared spectroscopy (FT-IR) and UV–visible spectrophotometry, Transmission Electron Microscopy (TEM), Scanning electron microscopy (SEM) along with X-ray energy dispersive spectroscopy (EDAX), and X-ray diffraction (XRD). The catalytic behaviour of the synthesized samples toward the reduction reaction of 4-nitrophenol in the presence of NaBH₄ was studied. It is indicated that the synthesized nanocomposites show a satisfactory catalytic activity. The catalytic reduction of p-NP to p-AP obeys first-order kinetics with rate constant in the following order (Ag-NP> (Ag/Co₃O₄-NC) ?1:1 > 1:3 > 3:1> Co₃O₄). This may be attributed to the high dispersion of Ag-NP compared to cobalt oxide nanoparticles. The microbial activity of the samples was analyzed using seven species of pathogenic microorganisms; 1) two species belongs to Gram negative bacteria; Escherichia coli (E.coli), and Salmonella, 2)four species belongs to Gram positive bacteria Marsa, Listeria, Staphylococcus aureus (S. aureus), bacillus subtilis (B.subtilis), and 3) one pathogenic fungal species Candidia. The data show that all samples exhibited an excellent range of inhibition toward all tested pathogenic microorganisms.     

Studies on Properties of Rice Straw/Polymer Nanocomposites Based on Polycaprolactone and Fe3O4 Nanoparticles and Evaluation of Antibacterial Activity

Modified rice straw/Fe₃O₄/polycaprolactone nanocomposites (ORS/Fe₃O₄/PCL-NCs) have been prepared for the first time using a solution casting method. The RS/Fe₃O₄-NCs were modified with octadecylamine (ODA) as an organic modifier. The prepared NCs were characterized by using X-ray powder diffraction (XRD), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), Thermogravimetric analysis (TGA) and Fourier transform infrared spectroscopy (FT-IR). The XRD results showed that as the intensity of the peaks decreased with the increase of ORS/Fe₃O₄-NCs content in comparison with PCL peaks, the Fe₃O₄-NPs peaks increased from 1.0 to 60.0 wt. %. The TEM and SEM results showed a good dispersion of ORS/Fe₃O₄-NCs in the PCL matrix and the spherical shape of the NPs. The TGA analysis indicated thermal stability of ORS/Fe₃O₄-NCs increased after incorporation with PCL but the thermal stability of ORS/Fe₃O₄/PCL-NCs decreased with the increase of ORS/Fe₃O₄-NCs content. Tensile strength was improved with the addition of 5.0 wt. % of ORS/Fe₃O₄-NCs. The antibacterial activities of the ORS/Fe₃O₄/PCL-NC films were examined against Gram-negative bacteria (Escherichia coli) and Gram-positive bacteria (Staphylococcus aureus) by diffusion method using nutrient agar. The results indicated that ORS/Fe₃O₄/PCL-NC films possessed a strong antibacterial activity with the increase in the percentage of ORS/Fe₃O₄-NCs in the PCL.     

Transmittance Measurements in Non-alternating Magnetic Field as Reliable Method for Determining of Heating Properties of Phosphate and Phosphonate Coated Fe3O4 Magnetic Nanoparticles

Different phosphates and phosphonates have shown excellent coating ability toward magnetic nanoparticles, improving their stability and biocompatibility which enables their biomedical application. The magnetic hyperthermia efficiency of phosphates (IDP and IHP) and phosphonates (MDP and HEDP) coated Fe₃O₄ magnetic nanoparticles (MNPs) were evaluated in an alternating magnetic field. For a deeper understanding of hyperthermia, the behavior of investigated MNPs in the non-alternating magnetic field was monitored by measuring the transparency of the sample. To investigate their theranostic potential coated Fe₃O₄-MNPs were radiolabeled with radionuclide ¹⁷⁷Lu. Phosphate coated MNPs were radiolabeled in high radiolabeling yield (>?99%) while phosphonate coated MNPs reached maximum radiolabeling yield of 78%. Regardless lower radiolabeling yield both radiolabeled phosphonate MNPs may be further purified reaching radiochemical purity of more than 95%. In vitro stabile radiolabeled nanoparticles in saline and HSA were obtained. The high heating ability of phosphates and phosphonates coated MNPs as sine qua non for efficient in vivo hyperthermia treatment and satisfactory radiolabeling yield justifies their further research in order to develop new theranostic agents.

     

Fabrication of Neodymium (Nd), Cadmium (Cd) and Nd:Cd doped hybrid copper oxide nanocomposites: Evaluation of their antibacterial activity and cytotoxicity against human L132 cell line

In the present study, Neodymium (Nd), Cadmium (Cd), and the various molar ratios of Nd: Cd doped copper oxide nanocomposites (CuO NCs) were prepared by the co-precipitation method. The as-synthesized Nd, Cd, and Nd:Cd doped CuO NCs [Cu_1-x + yNd_xCd_yO, (x:y = 0.006:0.00, 0.00:0.006, 0.005:0.001, 0.004:0.002, 0.003:0.003, M)] were characterized through various instrumentation techniques such as TGA, UV–Vis–NIR, FTIR, Raman, FL, XRD, ZP, FE-SEM with EDAX elemental mapping, HR-TEM and XPS analyses. Further, the antibacterial activity of doped CuO NCs was tested against Staphylococcus aureus and Escherichia coli. An equal molar ratio of Nd and Cd doped CuO NCs showed excellent antibacterial activity mainly due to the synergistic effect of sufficient Nd³⁺, Cd²⁺, and Cu²⁺ ions releasing ability. Interestingly, the doping effect enhances surface defects and decreases the ability to scavenge free radicals compared to pure CuO nanomaterials. At the same time, the cytotoxicity of NCs was evaluated on the human lung epithelial L132 cell line. Evidently, 75 μg/ml concentration of Nd:Cd doped CuO NCs samples shows 80% viability, which confirms their negligible cytotoxic effect. The Nd:Cd doped CuO NCs (94:3:3) had a high aspect ratio shape, remarkable ion-releasing ability, and biocompatibility while being thermally stable. Because of these qualities, they are well suited for treating bacterial infections in the biomedical area.     

Graphene nanoplatelets/Cr2O3 nanocomposites as novel nanoantibiotics: Towards control of multiple drug resistant bacteria

Drug resistance resulting due to the abuse of antibiotics can possibly be fatal for human beings. It, therefore, is required to develop novel nanoantibiotics to fight with the bacterial infections. In this work, we report graphene nanoplatelets/Cr₂O₃ nanocomposites (GNPs/Cr₂O₃) as a potential nanomedicine. Antibacterial characteristics of GNPs/Cr₂O₃ nanocomposites have been investigated against Pseudomonas aeruginosa and Staphylococcus aureus. GCr₂O₃-II with the optimized GNPs’ content shows excellent antibacterial performance with 84.25% growth inhibition of S. aureus (Gram-positive bacteria) and 80.76% growth inhibition of -P. aeruginosa (Gram-negative bacteria). This can be attributed to the synergistic contribution of Cr₂O₃ nanoflakes and GNPs/Cr₂O₃ nanocomposites, towards bacterial membrane disruption, that may be caused by the sharp edges of GNPs and induction of the oxidative stress by Cr₂O₃ nanoflakes. Therefore, this study suggests that GNPs/Cr₂O₃ nanocomposites can be employed as an innovative nanoantibiotics for pathogen control.     

Silica coating of Fe3O4 magnetic nanoparticles with PMIDA assistance to increase the surface area and enhance peptide immobilization efficiency

The high efficiency of using N-(phosphonomethyl)iminodiacetic acid (PMIDA) as a surfactant for formation of a silica coating on Fe₃O₄ magnetic nanoparticles (MNPs) with a large surface area has been demonstrated. The coating of PMIDA-stabilized MNPs with silica and their further APS-functionalization significantly increased the specific area (up to 203 m² g^?1) and the number of amino groups (up to 1.12 mmol/g) grafted on their surface compared to nanomaterials synthesized without preliminary SiO₂-coating. The comparative study of the peptide modification efficiency, using as an example pH-low insertion peptide (pHLIP), of MNPs coated with 3-aminopropylsilane (APS) or SiO₂/APS was carried out. It has been shown that silica coating of PMIDA-stabilized MNPs leads to a significant increase in the degree of immobilization of the peptide (up to 22 μmol per g of MNPs). Comprehensive characterization of the obtained materials at each stage of the synthesis was carried out using scanning electron microscopy (SEM), energy dispersive X-ray fluorescence spectroscopy (EDX), BET analysis, ATR Fourier transformed infrared spectroscopy (FTIR), termogravimetric analysis (TGA), CHN-elemental analysis, dynamic light scattering (DLS), and vibrating sample magnetometry (VSM). The proposed approach to applying SiO₂-coating of MNPs can be useful for design of new materials for biomedical and chemical purposes.     

Green synthesis,characterization and antimicrobial activity of carbon quantum dots-decorated ZnO nanoparticles

In this research, ZnO nanoparticles (ZnO NPs) and Carbon Quantum Dots-decorated ZnO nanoparticles (ZnO/CQDs NCs) were prepared via different procedures and precursors. Soya chunk was applied as a source of carbon for the preparation of CQDs. Crystalline structure, purity, size, and morphological properties of products were investigated via X-ray diffraction (XRD) analysis, energy dispersive spectroscopy (EDS), Transmission Electron Microscopy (TEM), FT-IR, and Scanning Electron Microscopy (SEM) respectively. Findings showed that homogeneity, size, and morphological properties of products can be intensively affected via different precursors and procedures. From the homogeneity, size, and morphological point of view, the hydrothermal route, ammonia, 5 h, and 180 °C were the optimum procedure, pH adjuster, temperature, and time respectively. Optimum product was applied for carrying out minimum inhibitory concentration (MIC) and Agar disk-diffusion tests against various microorganisms. Results demonstrated that prepared ZnO NPs have maximum antibacterial activity against Staphylococcus aureus (19.53 μg/ml) and ZnO/CQDs NCs have no inhibitory effect against tested microorganisms. For ZnO NPs, the disk diffusion test proved that the highest growth inhibition zone was related to Staphylococcus aureus (15 mm). The presence of CQDs in ZnO/CQDs NCs reduces the inhibitory effect of ZnO NPs intensively.     

The impact of Nb2O5 on in-vitro bioactivity and antibacterial activity of CaF2–CaO–B2O3–P2O5–SrO glass system

This work consists of in vitro bioactivity (in SBF) and antibacterial studies (against S. aureus and E. coli bacteria) of Nb₂O₅ doped bioactive glasses. X-ray diffraction and scanning electron microscopy investigations indicated deposition of Nb-HAp (hydroxyapatite) crystalline layer on the samples after exposing to SBF. The spectroscopy investigations also indicated the deposition of HAp layer on these samples. The magnitude of HAp deposited on the glasses found to be relying on concentration of Nb₂O₅ dopant; this conclusion was drawn by determining weight loss of the glasses due to exposure to SBF and also by assessing the variation of pH of the remnant fluid as functions of Nb₂O₅content. The studies further indicated the maximal content of hydroxyapatite was deposited on the surface the glasses doped with 4.0 mol% of Nb₂O₅. The antibacterial studies (against E. coli and S. aureus bacteria) of these glasses indicated the maximal killing effect of bacteria of the samples admixed with 4.0 mol% of Nb₂O₅. This result is attributed to the occupancy of maximal fraction of Nb ions in NbO₆ structural units (confirmed by IR and Raman spectroscopic results) in this sample that paved the way for easy disintegration of the glass and to act on the bacteria. Overall, the results of bioactivity studies of Nb₂O₅ doped bioglasses indicated that the Nb₂O₅ not only enhanced bioactivity potential but also exhibited antimicrobial activity.     

Preparation and Antibacterial Activity of Nano Copper Oxide- Loaded Zeolite 10X

Copper oxide nanosheet-loaded zeolite 10X nanocomposites (CuO-zeolite NCs) were successfully prepared by modifying zeolite 10X with CuSO₄ aqueous solution. The formation of copper oxide nanosheets on the surface of zeolite 10X was observed by SEM. The thickness of CuO nanosheets was about 30–40 nm, and the width ranged from 200 nm to 300 nm. The XRD patterns showed that the new diffraction peaks of copper oxide appeared at 35.6° and 38.8°. According to the XPS results, the Cu 2p_3/2 and Cu 2p_1/2 peaks in CuO-zeolite NC were centered at 934.1 eV and 953.8 eV, which could be attributed to Cu(II). The EDS analysis revealed that the energy spectra of calcium gradually decreased as the copper ion concentration increased during the preparation of CuO-zeolite NCs. Meanwhile, the energy spectra of copper increased gradually, and the highest content of copper in CuO-zeolite NCs reached 22.35 wt.%. The BET surface areas of zeolite 10X and CuO-zeolite NCs were 587 and 363 m²/g, respectively, based on the N₂ adsorption–desorption experiment. The antibacterial activities of CuO-zeolite NC were evaluated using Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). The antibacterial activities were related to both copper ion content in CuO-zeolite NCs and the particle size of copper oxide. The results showed that nano CuO-loaded zeolite 10X inhibited the activity of E. coli and S. aureus. CuO-zeolite NCs are expected to be further used in antifouling coating.     

A Self-Supplying H2O2 Modified Nanozyme-Loaded Hydrogel for Root Canal Biofilm Eradication

The success of root canal therapy depends mainly on the complete elimination of the root canal bacterial biofilm. The validity and biocompatibility of root canal disinfectant materials are imperative for the success of root canal treatment. However, the insufficiency of the currently available root canal disinfectant materials highlights that more advanced materials are still needed. In this study, a nanozyme-loaded hydrogel (Fe₃O₄-CaO₂-Hydrogel) was modified and analyzed as a root canal disinfectant material. Fe₃O₄-CaO₂-Hydrogel was fabricated and examined for its release profile, biocompatibility, and antibacterial activity against E. faecalis and S. sanguis biofilms in vitro. Furthermore, its efficiency in eliminating the root canal bacterial biofilm removal in SD rat teeth was also evaluated. The results in vitro showed that Fe₃O₄-CaO₂-Hydrogel could release reactive oxygen species (ROS). Moreover, it showed good biocompatibility, disrupting bacterial cell membranes, and inhibiting exopolysaccharide production (p < 0.0001). In addition, in vivo results showed that Fe₃O₄-CaO₂-Hydrogel strongly scavenged on root canal biofilm infection and prevented further inflammation expansion (p < 0.05). Altogether, suggesting that Fe₃O₄-CaO₂-Hydrogel can be used as a new effective biocompatible root canal disinfectant material. Our research provides a broad prospect for clinical root canal disinfection, even extended to other refractory infections in deep sites.     

Preparation and photocatalytic antibacterial mechanism of porous metastable β-Bi2O3 nanosheets

Effective and safe application of antibacterials has always been an important aspect for their usage. High-efficiency photocatalytic technology driven by visible light for antibacterial action constitutes a practical solution for antibacterial agents and will not harm the human body or the environment. While most studies on β-Bi₂O₃ materials with good photocatalytic properties under visible light are conducted in the field of optoelectronics, their potential and mechanism as photocatalytic antibacterial agents have not yet been fully explored. Herein, we report the performance of sheet-like metastable β-Bi₂O₃ material with rich oxygen vacancies and high electron-hole separation efficiency in antibacterial processes, as well as a preliminary exploration of its antibacterial mechanism. The results revealed that the antibacterial activity of the product against E. coli greatly improved in comparison with commercially available α-Bi₂O₃ owing to its excellent structure and optical properties. In addition, gradient experiments and scavenger experiments have confirmed that the main antibacterial effect of β-Bi₂O₃ originates from reactive oxygen species (ROS), and the superoxide radical, ·O₂⁻, of generated ROS is the key reactive species in the antibacterial process. Through the detection of lipid peroxidation and bacterial respiratory-chain dehydrogenase activity, several pathways were identified for the excellent antibacterial activity of the product.     

Synthesis and characterization of novel conducting composites of Fe3O4 nanoparticles and sulfonated polyanilines

Surface charged iron oxide (Fe₃O₄) nanoparticles were used for the synthesis of sulfonated polyaniline (SPAN)‐Fe₃O₄ nanocomposites (SPAN/Fe₃O₄‐NCs). 2,5‐diaminobenzenesulfonic acid (DABSA) and 2‐aminobenzenesulfonic acid (ABSA) were independently polymerized with aniline to form SPAN. The structure of the composites was characterized by means of transmission electron microscopy (TEM), X‐ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier transform infrared (FTIR) spectra, conductivity and magnetic properties. TEM reveals that Fe₃O₄ nanoparticles are “glued” with SPAN in the composite. TGA indicates that SPAN/Fe₃O₄‐NCs are having better thermal stability. The room temperature conductivity of SPAN/Fe₃O₄‐NCs is higher than that of pristine PANI and SPAN. SPAN/Fe₃O₄‐NCs exhibits magnetic behavior. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 4127–4134, 2007     

Use of magnetic and fluorescent polystyrene/tetraphenylporphyrin/maghemite nanocomposites for the photoinactivation of pathogenic bacteria

In this work, we initially describe the preparation of magnetic and fluorescent nanocomposites (MF NCs) based on polystyrene/tetraphenylporphyrin/maghemite (PS/TPP/γ-Fe₂O₃). After carrying a series of exploratory experiments, we have found that the composite that presented the highest values of fluorescence intensity and magnetization (S1 samples) was obtained when we employed 1 mL of TPP and 1% of PS. When tested as photosensitizer agents for the inactivation of the pathogenic bacteria Escherichia coli, these MF NCs presented excellent antibacterial activity, indicating that they can be promising candidates to inactivate microorganisms dispersed in aqueous solutions. Taking into account this peculiar combination of outstanding properties and simple and low cost synthesis, we suggest that this kind of NC could find widespread use in environmental and biomedical applications.     

Magnetically Separable Fe3O4 Nanoparticles-Decorated Reduced Graphene Oxide Nanocomposite for Catalytic Wet Hydrogen Peroxide Oxidation

Fe₃O₄ nanoparticles-decorated reduced graphene oxide magnetic nanocomposites (Fe₃O₄/rGO NCs) were prepared by a facile one-step strategy, and further used as heterogeneous Fenton-like catalysts for catalytic wet hydrogen peroxide oxidation (CWHPO) of methylene blue (MB) at 25 °C and atmospheric pressure. The effects of variables such as the Fe₃O₄/rGO with the mass ratio of rGO, initial pH, MB concentration and H₂O₂ dosage were investigated. The Fe₃O₄/rGO NCs with rGO mass ratio of 10.0 wt % showed the highest H₂O₂-activating ability, which was six-fold than that of pure Fe₃O₄ nanoparticles (NPs). The resulting catalysts demonstrated high catalytic activity in a broad operation pH range from 5 to 9, and still retained 90.5 % catalytic activity after reuse in five cycles. Taking advantage of the combined benefits of rGO and magnetic Fe₃O₄ NPs, these Fe₃O₄/rGO NCs were confirmed as an efficient heterogeneous Fenton-like catalyst for CWHPO to treat organic pollutants. And a reasonable catalytic mechanism of Fe₃O₄/rGO NCs was proposed to interpret the degradation process.     

Modification of chitosan-Fe3O4 microspheres with isophorone diisocyanate and formation of polyurethane/mchitosan-Fe3O4 antimicrobial polymer

Polyurethane/modified chitosan-Fe₃O₄ (PU/mCS-Fe₃O₄) nanocomposites were prepared by incorporating chitosan-Fe₃O₄ (CS-Fe₃O₄) into PU through chemical grafting using isophorone diisocyante (IPDI). The isocyanate group of IPDI was introduced on the surface of CS-Fe₃O₄ nanocomposites. The chemical functionalities of the CS-Fe₃O₄ and mCS-Fe₃O₄ were verified by Fourier-transform infrared and X-ray diffraction. The structure and properties were confirmed by scanning electron microscope, vibrating sample magnetometer, thermogravimetric analysis, atomic force microscope, and tensile testing. The experimental results indicate that thermal stability, tensile strength, and storage modulus of nanocomposites were improved with the increasing content of mCS-Fe₃O₄. Meanwhile, PU/mCS-Fe₃O₄ nanocomposites have less cytotoxicity and good antibacterial activities againstEscherichia coli and Staphylococcus aureus.     

Antibacterial effect and cell metabolic activity of Na2CaSi2O6, β-NaCaPO4, and β-NaCaPO4-SiO2 versus hydroxyapatite

Hydroxyapatite (Ca₅(PO₂)₃(OH)) is extensively used in diverse clinical applications because of its relatively simple synthesis protocol, low cost, and chemical similarity to the mineral component of bones and teeth. Some limitations regarding bioactivity and antibacterial activity have motivated changes in its structure and the development of alternative materials to achieve better performances as bioceramics. In this study, the antibacterial effect and cell metabolic activity of the main crystalline phases (Na₂CaSi₂O₆, β-NaCaPO₄, and β-NaCaPO₄−SiO₂) derived from the original 45S5 bioactive glass were evaluated and compared with those induced by a commercial powder of hydroxyapatite. Powder samples of Na₂CaSi₂O₆, β-NaCaPO₄, and β-NaCaPO₄−SiO₂ were synthesized by a simple and reproducible solid-state reaction method. The β-NaCaPO₄−SiO₂ sample exhibited the strongest effect against Pseudomonas aeruginosa, Staphylococcus aureus, and S. epidermidis, which are bacteria that normally colonize the skin but can become opportunistic pathogens when the host's resistance is low. All bacteria were eliminated within 5 min in the direct-contact test, an effect that is likely associated with changes in pH in the microenvironment generated from the partial solubilization of the material and the action of certain released ions, such as Ca²⁺. In vitro experiments with human cells, no sample showed cytotoxicity, and the β-NaCaPO₄−SiO₂ sample stood out once more inducing the most positive effect on keratinocyte and stem cell viability. Overall, the tested materials demonstrated similar or better (β-NaCaPO₄−SiO₂) biochemical properties than hydroxyapatite. This finding encourages us, and perhaps other research groups, to assess the bio-performance of these materials more comprehensively, aiming at the development of new products for use in tissue engineering.     

Synthesis,characterization, and corrosion inhibition study of polyaniline‐α‐Fe2O3 nanocomposite

Polyaniline (PANI)‐α‐Fe₂O₃ nanocomposites (NCs) have been synthesized by chemical oxidative in situ polymerization of aniline in presence of α‐Fe₂O₃ nanoparticles at 5°C using (NH₄)₂S₂O₈ as an oxidant in an aqueous solution of sodium dodecylbenzene sulphonic acid (SDBS), as surfactant and dopant under N₂ atmosphere. The room temperature conductivity of NCs decreases and coercive force (H_c) increases with an increase addition of α‐Fe₂O₃ in PANI matrix. The result of FTIR and TGA shows that the interaction between α‐Fe₂O₃ particles and PANI matrix could improve the thermal stability of NCs. NCs demonstrate the superparamagnetic behavior. The performance of PANI and PANI‐α‐Fe₂O₃ NCs as protective coating, against corrosion of 316LN stainless steel in 3.5% NaCl was assessed by potentiodynamic polarization technique. The study shows a good corrosion inhibition effect of both the coatings. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Hybrid Nanocomposites of Hydroxyapatite,Eu2O3, Graphene Oxide Via Ultrasonic Power: Microstructure,Morphology Design and Antibacterial for Biomedical Applications

Post-implantation infections are regarded as a major issue in the biomedical field. Further, many investigations are continuous towards developing antibacterial biocompatible materials. In this regard, hydroxyapatite (HAP), erbium oxide (Eu₂O₃), and graphene oxide (GO) were introduced in nanocomposites combinations, including single, dual, and triple constituents. The nanoparticles of HAP, Eu₂O₃, and nanosheets of GO are synthesized separately, while dispersed in the nanocomposites simultaneously. The morphological investigation showed that HAP was configured in a rod-like shape while the nano ellipsoidal shape of Eu₂O₃ was confirmed. The particle size of the ternary nanocomposite containing HAP/Eu₂O₃/GO reached the length of 40 nm for the rods of HAP and around 28 nm for the length axis of ellipsoidal Eu₂O₃ nanoparticles. The roughness average increased to be about 54.7 nm for HAP/GO and decreased to 37.9 nm for the ternary nanocomposite. Furthermore, the maximum valley depth (R_v) increased from HAP to the ternary nanocomposite from 188.9 to 189.8 nm. Moreover, the antibacterial activity was measured, whereas the inhibition zone of HAP/Eu₂O₃/GO reached 13.2?±?1.1 mm for Escherichia coli and 11.4?±?0.8 mm for Staphylococcus aureus. The cell viability of the human osteoblast cell lines was evaluated to be 98.5?±?3% for the ternary composition from 96.8?±?4% for the pure HAP. The existence of antibacterial activity without showing cytotoxicity against mammalian cells indicates the compatibility of nanocomposites with biomedical applications.

     

Antibacterial activity and corrosion resistance of Ta2O5 thin film and electrospun PCL/MgO-Ag nanofiber coatings on biodegradable Mg alloy implants

Biodegradable magnesium (Mg) alloys have drawn considerable attention for use in orthopedic implants, but their antibacterial activity and corrosion resistance still require improvement. In the present work, functional Ta₂O₅ (tantalum pentoxide) compact layers and PCL/MgO-Ag (poly (ε-caprolactone)/magnesium oxide-silver) nanofiber porous layers were subsequently deposited on Mg alloys via reactive magnetron sputtering and electrospinning, respectively, to improve anticorrosion and antibacterial performance. Sputter coating of the Ta₂O₅ resulted in a thick layer (～1?μm) with an amorphous structure and high adhesive strength. The nanostructure exhibited bubble-like patterns with no obvious nano-cracks, nano-porosities, or pinholes. The electrospun PCL/MgO-Ag nanofiber coating was porous, smooth, and plain with no obvious beads. In vitro corrosion tests demonstrated the PCL/MgO-Ag nanofiber-coated alloy had greater corrosion resistance than a Ta₂O₅ sputter-coated alloy or uncoated Mg alloy. The additional electrospun PCL/MgO-Ag nanofiber coating also had greater antibacterial behavior toward Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria than the Ta₂O₅-coated or uncoated alloy specimens. Increasing the MgO-Ag concentration of the nanofibers from 1 to 3?wt% increased antibacterial activity. The combination of Ta₂O₅ and PCL/MgO-Ag nanofiber coatings on Mg alloys may therefore have potential applications for reducing bone infection as related to orthopedic implants for bone repair.     

Preparation and characterization of SiO2/polydopamine/Ag nanocomposites with long-term antibacterial activity

Silver nanoparticles (Ag NPs) with diameter of approximately 10 nm were prepared by the reduction of silver nitrate using green synthesis, an eco-friendly approach. The synthesized Ag NPs were homogeneously deposited on silicon dioxide (SiO₂) particles modified with dopamine, leading to the formation of SiO₂/polydopamine (PD)/Ag nanocomposites (NCs) with a core–shell–satellite structure investigated by transmission electron microscopy. The Ag content of SiO₂/PD/Ag NCs determined by inductively coupled plasma optical emission spectrometry was approximately 5.92 wt%. The antibacterial properties of both Ag NPs and SiO₂/PD/Ag NCs against Vibrio natriegens (V. natriegens) and Erythrobacter pelagi sp. nov. (E. pelagi) were investigated by bacterial growth curves and inhibition zone. Compared to Ag NPs, the SiO₂/PD/Ag NCs exhibited superior long-term antibacterial activity, attributed to its controlled release of Ag⁺ ions.